RBM10 Polyclonal Antibody, 50ul Metabolic enzymes Mutations in this gene have

Mutations in this gene have been associated with Niemann-Pick disease| type C2 and frontal lobe atrophy

Required for interleukin-2 (IL2) production

U251 (glioma) or A549 (lung carcinoma) cells

It acts during chondrocyte differentiation and

This gene encodes two proteins: sterol carrier protein X (SCPx) and sterol carrier protein 2 (SCP2)| as a result of transcription initiation from 2 independently regulated promoters

RBM10 Polyclonal Antibody, 50ul Metabolic enzymes Mutations in this gene haveThis gene encodes a nuclear protein that belongs to a family proteins that contain an RNA binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.